{"title":"地中海贫血患者错牙合","authors":"Mohamad Azhar Ibrahim Kharsa","doi":"10.15761/DOMR.1000350","DOIUrl":null,"url":null,"abstract":"This case report is to present two cases of young boys with β thalassemia, have skeletal class II convex profile, protrusion of the maxilla and mandible, protrusion of the upper incisors and smaller incisor widths. Cephalometric x-ray shows overgrowth of the maxilla bone, with presence of bone voids and hiatuses. The treatment of patients with β thalassemia is usually controversy, require good diagnosis, investigations and treatment plan.","PeriodicalId":10996,"journal":{"name":"Dental, Oral and Maxillofacial Research","volume":"85 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Thalassemia patients with malocclusion\",\"authors\":\"Mohamad Azhar Ibrahim Kharsa\",\"doi\":\"10.15761/DOMR.1000350\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This case report is to present two cases of young boys with β thalassemia, have skeletal class II convex profile, protrusion of the maxilla and mandible, protrusion of the upper incisors and smaller incisor widths. Cephalometric x-ray shows overgrowth of the maxilla bone, with presence of bone voids and hiatuses. The treatment of patients with β thalassemia is usually controversy, require good diagnosis, investigations and treatment plan.\",\"PeriodicalId\":10996,\"journal\":{\"name\":\"Dental, Oral and Maxillofacial Research\",\"volume\":\"85 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Dental, Oral and Maxillofacial Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.15761/DOMR.1000350\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Dental, Oral and Maxillofacial Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15761/DOMR.1000350","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
This case report is to present two cases of young boys with β thalassemia, have skeletal class II convex profile, protrusion of the maxilla and mandible, protrusion of the upper incisors and smaller incisor widths. Cephalometric x-ray shows overgrowth of the maxilla bone, with presence of bone voids and hiatuses. The treatment of patients with β thalassemia is usually controversy, require good diagnosis, investigations and treatment plan.